Literature DB >> 15180033

Mitochondrial encephalomyopathy with lactic acidosis and strokelike episodes (MELAS): a mitochondrial disorder presents as fibromyalgia.

Rowena A DeSouza1, Raul J Cardenas, Tekisha U Lindler, Francisco A De la Fuente, Francisco J Mayorquin, David S Trochtenberg.   

Abstract

This case report describes a patient who presented with symptoms and signs of longstanding fibromyalgia. Routine laboratory tests revealed an elevated anion gap. Evaluation of the elevated anion gap demonstrated elevated lactate and pyruvate levels and a lactate-to-pyruvate ratio greater than 20:1. A muscle biopsy was performed, exhibiting red ragged fibers, pathognomonic for a mitochondrial disorder. The patient was diagnosed with mitochondrial encephalomyopathy with lactic acidosis and strokelike episodes (MELAS). This is the first report describing fibromyalgia as the initial presentation of MELAS. This article outlines the diagnostic process that can assist the physician in distinguishing mitochondrial disorders from other muscular diseases, particularly fibromyalgia.

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Year:  2004        PMID: 15180033     DOI: 10.1097/00007611-200405000-00023

Source DB:  PubMed          Journal:  South Med J        ISSN: 0038-4348            Impact factor:   0.954


  3 in total

1.  Charles Darwin's mitochondria.

Authors:  John Hayman
Journal:  Genetics       Date:  2013-05       Impact factor: 4.562

2.  Involvement of TRPM2 and TRPV1 channels on hyperalgesia, apoptosis and oxidative stress in rat fibromyalgia model: Protective role of selenium.

Authors:  Esra Yüksel; Mustafa Nazıroğlu; Mehmet Şahin; Bilal Çiğ
Journal:  Sci Rep       Date:  2017-12-13       Impact factor: 4.379

3.  A descriptive pilot study of mitochondrial mutations & clinical phenotype in fibromyalgia syndrome.

Authors:  Sumita Danda; Blessy Mariam Thomas; G Paramasivam; Raji Thomas; John Mathew; Debashish Danda
Journal:  Indian J Med Res       Date:  2019-01       Impact factor: 2.375

  3 in total

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